An ammonia-containing tail gas absorption system, comprising at least two sets of absorption devices, wherein at least two transport pipelines are provided at inlets of some of the absorption devices, and the transport pipelines are used to communicate the absorption devices with an ammonia-containing tail gas outlet of a reactor or other absorption devices. Valves are provided on the transport pipelines, and the valves are used to control the connection and disconnection of the transport pipelines so as to switch the series-parallel relationship between the sets of absorption devices.

An ammonia-containing tail gas absorption system, comprising at least two sets of absorption devices, wherein at least two transport pipelines are provided at inlets of some of the absorption devices, and the transport pipelines are used to communicate the absorption devices with an ammonia-containing tail gas outlet of a reactor or other absorption devices. Valves are provided on the transport pipelines, and the valves are used to control the connection and disconnection of the transport pipelines so as to switch the series-parallel relationship between the sets of absorption devices.

An ammonia chemical species desorption process desorbs ammonia chemical species adsorbed onto a Prussian blue derivative more simply at lower cost under milder conditions as compared with using an aqueous solution of a salt or strong acid, and only water. This ammonia chemical species desorption process includes an ammonia chemical desorption step of bringing carbon dioxide and water into contact with a Prussian blue derivative represented by the following general formula (1), thereby desorbing an ammonia chemical species.

A.sub.xM[M′(CN).sub.6].sub.y.zH.sub.2O  (1)

where x is 0 to 3, y is 0.1 to 1.5, z is 0 to 6, A is at least one cation of hydrogen, ammonium, an alkaline metal, and an alkaline earth metal, and M and M′ are each independently at least one cation of at least one of atoms having atomic numbers 3 to 83 except for ammonium, an alkali metal, and an alkaline earth metal.

A method for liquefying ammonia can include the steps of: providing a pressurized carbon dioxide stream from a power generating facility; expanding the pressurized carbon dioxide stream to a lower pressure that is sufficient to produce a dual phase carbon dioxide fluid; introducing the dual phase carbon dioxide fluid to a gas-liquid separator; withdrawing a liquid stream from the gas-liquid separator; and liquefying an ammonia gas stream in an ammonia liquefier by indirect contact with the liquid stream from the gas-liquid separator, thereby forming a liquid ammonia stream and a gaseous carbon dioxide stream.

An ammonia decomposition facility includes a heating medium line configured to flow a heating medium heated by heat generated by a gas turbine, an ammonia supply line configured to flow ammonia, an ammonia decomposition device, and an ammonia removal device. The ammonia decomposition device is configured to use heat of the heating medium from the heating medium line, thermally decompose ammonia from the ammonia supply line, and generate a decomposition gas containing hydrogen, nitrogen, and residual ammonia. The ammonia removal device is configured to remove the residual ammonia contained in the decomposition gas from the ammonia decomposition device.

An object of the present invention to provide a method for producing methionine with consideration given to the environment. The production method of the present invention comprises a removal step of blowing an inert gas into a liquid containing 5-(2-methylmercaptoethyl)hydantoin and thereby diffusing ammonia remaining in the liquid to obtain an emission gas containing the ammonia, and a recovery step of bringing the emission gas into contact with a washing liquid to recover ammonia contained in the emission gas.

The present invention discloses methods for extracting and recycling ammonia in MOCVD processes by FTrPSA. Through pretreatment, medium-shallow temperature PSA concentration, condensation and freezing, liquid ammonia vaporization, PSA ammonia extraction, and ammonia gas purification procedures, ammonia-containing exhaust gases from MOCVD processes are purified to meet the electronic-level ammonia gas standard required by the MOCVD processes, so as to implement recycling and reuse of the exhaust gases, where the ammonia gas yield is greater than or equal to 70-85%. The present invention solves the technical problem that atmospheric-pressure or low-pressure ammonia-containing exhaust gases in MOCVD processes cannot be returned to the MOCVD processes for use after being recycled, and fills the gap in green and circular economy development of the LED industry.

The present invention discloses methods for extracting and recycling ammonia in MOCVD processes by FTrPSA. Through pretreatment, medium-shallow temperature PSA concentration, condensation and freezing, liquid ammonia vaporization, PSA ammonia extraction, and ammonia gas purification procedures, ammonia-containing exhaust gases from MOCVD processes are purified to meet the electronic-level ammonia gas standard required by the MOCVD processes, so as to implement recycling and reuse of the exhaust gases, where the ammonia gas yield is greater than or equal to 70-85%. The present invention solves the technical problem that atmospheric-pressure or low-pressure ammonia-containing exhaust gases in MOCVD processes cannot be returned to the MOCVD processes for use after being recycled, and fills the gap in green and circular economy development of the LED industry.

Provided is a method for separating ammonia gas using zeolite membrane having excellent separation stability at a high temperature capable of separating ammonia gas from a mixed gas composed of multiple components including ammonia gas, hydrogen gas, and nitrogen gas to the permeation side with high selectivity and high permeability. Also provided is a method for separating ammonia by selectively permeating ammonia gas from a mixed gas containing at least ammonia gas, hydrogen gas, and nitrogen gas using a zeolite membrane, wherein the ammonia gas concentration in the mixed gas is 1.0% by volume or more.

A high-temperature solid oxide fuel cell arrangement fueled by a hydrogen or hydrocarbon fuel and generating electricity and anunonia as a byproduct comprises: (a) a cathode area fed with a humid air; (b) an anode area fed with the fuel; and (c) an oxygen-conducting electrolyte disposed between the cathode and anode areas. The cathode has an ammonia-rich tail-gas stream. The fuel cell further comprises a gas separator configured for separating ammonia generated on the cathode from tail-gas stream and means for utilizing separated ammonia selected from the group consisting of: an ammonia reformer configured for generating hydrogen to be admixed to the fuel fed to the anode, a collecting tank for storing the anunonia and an auxiliary solid oxide fuel cell fueled by the separated anunonia and any combination thereof.